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肝细胞和线粒体中来自[1-¹⁴C]、[U-¹⁴C]和[16-¹⁴C]-棕榈酸酯的标记氧化产物。

Labeled oxidation products from [1-14C], [U-14C] and [16-14C]-palmitate in hepatocytes and mitochondria.

作者信息

Chatzidakis C, Otto D A

机构信息

Graduate Program in Nutrition, Rutgers, State University of New Jersey, New Brunswick.

出版信息

Lipids. 1987 Sep;22(9):620-6. doi: 10.1007/BF02533939.

Abstract

When [1-14C], [U-14C], and [16-14C]palmitate were oxidized by isolated rat hepatocytes, there was a differential distribution of label as a percent of total oxidized products, such that 14CO2 from [1-14C] greater than [U-14C] greater than [16-14C]palmitate and acid-soluble radioactivity from [16-14C] greater than [U-14C] greater than [1-14C]palmitate. The oxidation of [2,3-14C]succinate to 14CO2 by isolated hepatocytes was only 9.1% of that from [1,4-14C]succinate, demonstrating that the differences in distribution of labeled products are in part due to less 14CO2 production from label in the even carbon positions entering the citric acid cycle. Apparent total ketone body production from [16-14C]palmitate was markedly higher than [1-14C] and [U-14C]palmitate. In addition, the 14C-acetone:14CO2 ratio derived from decarboxylation of labeled acetoacetate from [1-14C]palmitate was less than 1 and positively correlated to the rate of fatty acid oxidation in hepatocytes. These findings indicate that the known preferential incorporation of the omega-C2 unit of fatty acids into 14C-ketone bodies also contributed to the differential distribution of labeled products and that this contribution was greatest at the lower rates of fatty acid oxidation. In isolated mitochondria, the distribution of label to 14CO2 and acid-soluble radioactivity from [1-14C], [U-14C] and [16-14C]palmitate was qualitatively similar to that seen with hepatocytes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

当[1-¹⁴C]、[U-¹⁴C]和[16-¹⁴C]棕榈酸酯被分离的大鼠肝细胞氧化时,作为总氧化产物百分比的标记物存在差异分布,使得来自[1-¹⁴C]棕榈酸酯的¹⁴CO₂大于[U-¹⁴C]棕榈酸酯大于[16-¹⁴C]棕榈酸酯,且来自[16-¹⁴C]棕榈酸酯的酸溶性放射性大于[U-¹⁴C]棕榈酸酯大于[1-¹⁴C]棕榈酸酯。分离的肝细胞将[2,3-¹⁴C]琥珀酸氧化为¹⁴CO₂的量仅为[1,4-¹⁴C]琥珀酸的9.1%,这表明标记产物分布的差异部分是由于进入柠檬酸循环的偶数碳位置的标记物产生的¹⁴CO₂较少。[16-¹⁴C]棕榈酸酯的表观总酮体生成量明显高于[1-¹⁴C]和[U-¹⁴C]棕榈酸酯。此外,[1-¹⁴C]棕榈酸酯标记的乙酰乙酸脱羧产生的¹⁴C-丙酮:¹⁴CO₂比值小于1,且与肝细胞中脂肪酸氧化速率呈正相关。这些发现表明,已知脂肪酸的ω-C₂单元优先掺入¹⁴C-酮体也导致了标记产物的差异分布,并且这种贡献在较低的脂肪酸氧化速率下最大。在分离的线粒体中,[1-¹⁴C]、[U-¹⁴C]和[16-¹⁴C]棕榈酸酯的标记物在¹⁴CO₂和酸溶性放射性中的分布在质量上与肝细胞中的相似。(摘要截短至250字)

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